×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Synchronous Onset of Breast and Pancreatic Cancers: Results of Germline and Somatic Genetic Analysis.
27721756 2019
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Genomic Heterogeneity Within Individual Prostate Cancer Foci Impacts Predictive Biomarkers of Targeted Therapy.
29398457 2019
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients.
29297111 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.29339979 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.
29335924 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
29394989 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
29371908 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
29446198 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
29394989 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Germline BRCA mutations in Asian patients with pancreatic adenocarcinoma: a prospective study evaluating risk category for genetic testing.
28782087 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Detection of Germline Mutations in Patients with Epithelial Ovarian Cancer Using Multi-gene Panels: Beyond BRCA1/2.
29020732 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Germline DNA-repair Gene Mutations and Outcomes in Men with Metastatic Castration-resistant Prostate Cancer Receiving First-line Abiraterone and Enzalutamide.
29439820 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan.
29176636 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia.
28528518 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.
29335924 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Germline mutation prevalence in individuals with pancreatic cancer and a history of previous malignancy.
29360161 2018
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
A high frequency of PALB2 mutations in Jamaican patients with breast cancer.
28194609 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
The First Nationwide Multicenter Prevalence Study of Germline BRCA1 and BRCA2 Mutations in Chinese Ovarian Cancer Patients.
28692638 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas.
27767231 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
GeneticVariation
CLINVAR
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort.
27495310 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer.
28024868 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Retesting BRCA1/BRCA2 mutation negative male breast cancer patients using next generation sequencing technologies.
28091860 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Malignant Brenner tumor associated with a germline BRCA2 mutation.
28616458 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?
29161300 2017
×
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
Neoplastic Syndromes, Hereditary
0.130
CausalMutation
CLINVAR
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
28423363 2017